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用一种新型单克隆抗体在石蜡切片上鉴定组织组织细胞

Identification of tissue histiocytes on paraffin sections by a new monoclonal antibody.

作者信息

Flavell D J, Jones D B, Wright D H

机构信息

University Department of Pathology, Southampton General Hospital, United Kingdom.

出版信息

J Histochem Cytochem. 1987 Nov;35(11):1217-26. doi: 10.1177/35.11.3309045.

DOI:10.1177/35.11.3309045
PMID:3309045
Abstract

A mouse monoclonal antibody (MAC 387) with specificity for monocytes and tissue histiocytes was produced by immunization of a BALB/c mouse with peripheral blood monocyte components derived by affinity chromatography of detergent-solubilized monocyte material on Sepharose 4B coupled to rabbit anti-monocyte antibodies. MAC 387 strongly stained the cytoplasm of cells of the monocyte/macrophage series on paraffin sections after controlled trypsinization of sections. The antibody showed broad reactivity for a variety of tissue histiocytes, including infiltrating and reactive histiocytes, alveolar macrophages, Kupffer cells, follicle-center macrophages, splenic red pulp macrophages, tumor-infiltrating macrophages, sinus histiocytes, epithelioid giant cells (variably), and cases of histiocytosis X and dermatopathic lymphadenopathy. Molecular weight data obtained by Western blotting, immunoprecipitation, and immunoaffinity-purification revealed that the antigen was present in different forms in the monocyte and granulocyte. In the granulocyte, free alpha (Mr 12 KD) and beta (Mr 14 KD) chains expressing the MAC 387 epitope were found together with associations of one alpha and one beta chain linked by disulfide bonds to yield a heterodimer of Mr 26 KD. In the monocyte, free alpha and beta chains are not found, but instead the heterodimer and associations of two (Mr 56 KD) and four (Mr 112 KD) heterodimers are disulfide-linked together. This new monoclonal reagent should have particular value for identification of tissue histiocytes in routine paraffin sections and particularly for demonstration of histiocytes in malignant lymphomas.

摘要

通过用经去污剂溶解的单核细胞材料在偶联有兔抗单核细胞抗体的琼脂糖4B上进行亲和层析得到的外周血单核细胞成分免疫BALB/c小鼠,制备了一种对单核细胞和组织组织细胞具有特异性的小鼠单克隆抗体(MAC 387)。在对切片进行可控胰蛋白酶消化后,MAC 387在石蜡切片上强烈染色单核细胞/巨噬细胞系列细胞的细胞质。该抗体对多种组织组织细胞具有广泛的反应性,包括浸润性和反应性组织细胞、肺泡巨噬细胞、库普弗细胞、滤泡中心巨噬细胞、脾红髓巨噬细胞、肿瘤浸润巨噬细胞、窦组织细胞、上皮样巨细胞(程度不一)以及组织细胞增生症X和皮肤性淋巴结病的病例。通过蛋白质印迹法、免疫沉淀法和免疫亲和纯化获得的分子量数据表明,该抗原在单核细胞和粒细胞中以不同形式存在。在粒细胞中,发现表达MAC 387表位的游离α链(分子量12 KD)和β链(分子量14 KD)以及一条α链和一条β链通过二硫键连接形成的分子量为26 KD的异二聚体。在单核细胞中,未发现游离的α链和β链,而是异二聚体以及两个(分子量56 KD)和四个(分子量112 KD)异二聚体通过二硫键连接在一起。这种新的单克隆试剂对于在常规石蜡切片中鉴定组织组织细胞,特别是在恶性淋巴瘤中显示组织细胞具有特殊价值。

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